Madhavan, L., 		Nagarajan, H., 		Vetrivel, U., & 		Jagadeesan, M.
(2024).
 In Silico Characterization of Two Adjacent Novel Homozygous Nucleotide Variations in the PEX6 Gene Predict L898V Mutation to Enhance Infantile Refsum Disease and Heimler Syndrome.
<em>Medical Research Archives, 12</em>(11).
doi:10.18103/mra.v12i11.5942